Abstract
Eight patients with severe rhesus disease and expected fetal loss were treated by intensive plasmapheresis using a continuous-flow cell separator. Plasmapheresis was started at 16-27 weeks' gestation, and continued until planned intrauterine transfusion or until the infant was delivered or the rhesus disease became uncontrolled again. Altogether 24 to 2371 of plasma was exchanged over periods ranging from seven to 16 weeks. In seven of the eight patients the anti-D concentration fell during the period of plasmapheresis. Amniotic fluid spectrophotometry values remained below those recorded in the preceding pregnancy in six out of seven women. In five patients an attempt was made to control the rhesus disease by plasmapheresis alone, and two of these women delivered infants who survived. In the other three cases the infants died, one from the idiopathic respiratory distress syndrome and the other two in utero. These preliminary findings suggest that intensive plasmapheresis with a cell separator may reduce fetal haemolysis is delivered. Nevertheless, plasmapheresis may best be used to reduce haemolysis until intrauterine transfusions may be given more safely after 30 weeks' gestation.
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Selected References
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- Clarke C. A., Elson C. J., Bradley J., Donohoe W. T., Lehane D., Hughes-Jones N. C. Intensive plasmapheresis as a therapeutic measure in Rhesus-immunised women. Lancet. 1970 Apr 18;1(7651):793–798. doi: 10.1016/s0140-6736(70)92406-2. [DOI] [PubMed] [Google Scholar]
- Fraser I. D., Bothamley J. E., Bennett M. O., Airth G. R. Intensive antenatal plasmapheresis in severe rhesus isoimmunisation. Lancet. 1976 Jan 3;1(7949):6–8. doi: 10.1016/s0140-6736(76)92906-8. [DOI] [PubMed] [Google Scholar]
- Fraser I. D., Tovey G. H., Lockyer W. J., Sobey D. F. Antibody protein levels in the maternal serum in rhesus iso-immunization. J Obstet Gynaecol Br Commonw. 1972 Dec;79(12):1074–1079. doi: 10.1111/j.1471-0528.1972.tb11888.x. [DOI] [PubMed] [Google Scholar]
- Holt E. M., Boyd I. E., Dewhurst C. J., Murray J., Naylor C. H., Smitham J. H. Intrauterine tranfusion: 101 consecutive cases treated at Queen Charlotte's Maternity Hospital. Br Med J. 1973 Jul 7;3(5870):39–43. doi: 10.1136/bmj.3.5870.39. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hughes-Jones N. C. The estimation of the concentration and equilibrium constant of anti-D. Immunology. 1967 May;12(5):565–571. [PMC free article] [PubMed] [Google Scholar]
- Logan R. W., Tweedie A. K. An evaluation of the SMA 12-micro autoanalyzer in the clinical biochemistry laboratory. Clin Chim Acta. 1973 Feb 28;44(1):73–83. doi: 10.1016/0009-8981(73)90162-9. [DOI] [PubMed] [Google Scholar]
- Marsh W. L., Nichols M., Jenkins W. J. Automated detection of blood group antibodies. J Med Lab Technol. 1968 Oct;25(4):335–342. [PubMed] [Google Scholar]
- Oon C. J., Hobbs J. R. Clinical applications of the continuous flow blood separator machine. Clin Exp Immunol. 1975 Apr;20(1):1–16. [PMC free article] [PubMed] [Google Scholar]
- Pole J. R., Barr W., Willoughby M. L. Letter: Continuous-flow exchange-plasmapheresis in severe rhesus isoimmunisation. Lancet. 1974 May 25;1(7865):1051–1051. doi: 10.1016/s0140-6736(74)90446-2. [DOI] [PubMed] [Google Scholar]
- Tovey L. A., Haggas W. K. Prediction of the severity of rhesus haemolytic disease by means of antibody titrations performed on the Autoanalyzer. Br J Haematol. 1971 Jan;20(1):25–33. doi: 10.1111/j.1365-2141.1971.tb00783.x. [DOI] [PubMed] [Google Scholar]
